Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Magnus W. Walter"'
Publikováno v:
Green Chemistry. 24:1469-1473
Simple use of KOH allows the direct F to OH exchange of aromatic and heteroaromatic substrates under mechanochemical conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::013ad39e1f626fa802003908e093d032
https://doi.org/10.1039/d1gc04361g
https://doi.org/10.1039/d1gc04361g
α-Amido trifluoromethyl alcohols and ketones were synthesised via two independent routes using the Ruppert Reagent (TMS-CF 3 ) and shown to be inhibitors of metallo-β-lactamases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27090b4c6262da94efa82238abacde2b
https://ora.ox.ac.uk/objects/uuid:b20952f2-511c-4030-b416-f10fe2ef6d8a
https://ora.ox.ac.uk/objects/uuid:b20952f2-511c-4030-b416-f10fe2ef6d8a
(Trifluoromethyl)trimethylsilane (TMS-CF3, the Ruppert Reagent) reacts with a variety of amino acid derived N-substituted oxazolidin-5-ones in excellent yields. Mild acid hydrolysis of adducts with electron-releasing substituents at C-2 affords N-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0118b943b1c947db87dc25fbe4e42b07
https://ora.ox.ac.uk/objects/uuid:300b66f6-5625-4e79-a73b-737735105e44
https://ora.ox.ac.uk/objects/uuid:300b66f6-5625-4e79-a73b-737735105e44
Autor:
Russell J. Cox, Roger V. Bonnert, Varinder K. Aggarwal, Bettina Bressel, Magnus W. Walter, Javier de Vicente, Jon Shepherd, Caroline L. Winn, Luke A. Adams, William G. Whittingham
Publikováno v:
The Journal of Organic Chemistry. 68:9433-9440
A simple and high-yielding method for the preparation of cyclopropane amino acids is described. The novel method involves the one-pot cyclopropanation of readily available dehydroamino acids using aryl and unsaturated diazo compounds generated in sit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2cb5b4cede833b7ce565cebc794055c
https://doi.org/10.1021/jo035060c
https://doi.org/10.1021/jo035060c
Autor:
Catherine A. McAdam, Mark G. McLaughlin, Magnus W. Walter, Adam J. S. Johnston, Matthew J. Cook, Jun Chen
Publikováno v:
ChemInform. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e46f146282c36eca0f583489491bd3f
https://doi.org/10.1002/chin.201344184
https://doi.org/10.1002/chin.201344184
Publikováno v:
ChemInform. 28
α-Amido trifluoromethyl alcohols and ketones were synthesised via two independent routes using the Ruppert Reagent (TMS-CF 3 ) and shown to be inhibitors of metallo-β-lactamases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::875e5fac24d7b3e82f4c8836d58d80bb
https://doi.org/10.1002/chin.199742231
https://doi.org/10.1002/chin.199742231
Publikováno v:
ChemInform. 29
(Trifluoromethyl)trimethylsilane (TMS-CF3, the Ruppert Reagent) reacts with a variety of amino acid derived N-substituted oxazolidin-5-ones in excellent yields. Mild acid hydrolysis of adducts with electron-releasing substituents at C-2 affords N-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c71295906a297de886382366f8e31a4
https://doi.org/10.1002/chin.199850080
https://doi.org/10.1002/chin.199850080
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::413968cd60d445798acd37bda1aa4167
https://doi.org/10.1002/chin.200018280
https://doi.org/10.1002/chin.200018280
Autor:
Magnus W. Walter, Jack E. Baldwin, John E. Moses, Serena J. Eade, Raphaël Rodriguez, Robert M. Adlington
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90456dabc8655417a077ee1093207207
https://doi.org/10.1002/chin.200735216
https://doi.org/10.1002/chin.200735216
Publikováno v:
Organic letters. 7(17)
As part of our continuing studies of pyrone-containing natural products, a series 6-methoxypyran-2-ones were synthesized. These were found to react with molecular oxygen at 20 degrees C, and this novel reaction yielded a series of highly functionaliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00e9300d1960dc657a2de97b88cf3fce
https://pubmed.ncbi.nlm.nih.gov/16092855
https://pubmed.ncbi.nlm.nih.gov/16092855